A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6135121



Internal ID8799846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9404062..9407134hg38UCSC Ensembl
Outerchr18:9403905..9407300hg38UCSC Ensembl
Innerchr18:9404060..9407132hg19UCSC Ensembl
Outerchr18:9403903..9407298hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg383396
hg193396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670362
Supporting Variants
SamplesHG00246
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6135121
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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